Search results for "SURFACE MODIFICATION"

showing 10 items of 417 documents

Easy Route to Functionalize Iron Oxide Nanoparticles via Long-Term Stable Thiol Groups

2009

International audience; The functionalization of superparamagnetic iron oxide nanoparticles (SPIOs) by meso-2,3-dimercaptosuccinic acid (DMSA) was investigated. Under ambient conditions, the thiol groups from DMSA are not stable and do not allow a direct functionalization without storage in stringent conditions or a chemical regeneration of free thiols. In this study, we have developed a protocol based on poly(ethylene glycol) (PEG) grafting of SPIO prior to DMSA anchoring. We have observed that PEG helps to increase the stability of thiol groups under ambient conditions. The thiol functionalized SPIOs were stable under physiological pH and ionic strength as determined by Ellman's essay and…

Inorganic chemistryIron oxide02 engineering and technology010402 general chemistryFerric Compounds01 natural scienceschemistry.chemical_compoundPEG ratioElectrochemistryReactive dyeGeneral Materials ScienceSulfhydryl CompoundsSpectroscopychemistry.chemical_classificationMolecular Structure[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry[CHIM.MATE]Chemical Sciences/Material chemistrySurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter PhysicsCombinatorial chemistry0104 chemical sciencesModels ChemicalchemistryIonic strength[ CHIM.MATE ] Chemical Sciences/Material chemistryThiolNanoparticlesSurface modificationSuccimer0210 nano-technologyEthylene glycolIron oxide nanoparticlesLangmuir
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Size and Surface Chemistry Tuning of Silicon Carbide Nanoparticles.

2017

International audience; Chemical transformations on the surface of commercially available 3C-SiC nanoparticles were studied by means of FTIR, XPS, and temperature-programmed desorption mass spectrometry methods. Thermal oxidation of SiC NPs resulted in the formation of a hydroxylated SiO2 surface layer with C3Si–H and CHx groups over the SiO2/SiC interface. Controllable oxidation followed by oxide dissolution in HF or KOH solution allowed the SiC NPs size tuning from 17 to 9 nm. Oxide-free SiC surfaces, terminated by hydroxyls and C3Si–H groups, can be efficiently functionalized by alkenes under thermal or photochemical initiation. Treatment of SiC NPs by HF/HNO3 mixture produces a carbon-e…

Inorganic chemistry[ SPI.MAT ] Engineering Sciences [physics]/MaterialsOxideNanoparticle02 engineering and technology010402 general chemistry01 natural sciences[SPI.MAT]Engineering Sciences [physics]/Materialschemistry.chemical_compoundX-ray photoelectron spectroscopystomatognathic systemDesorptionElectrochemistryGeneral Materials ScienceSurface layer[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsSpectroscopy[PHYS]Physics [physics]Thermal oxidation[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Aqueous solution[ PHYS ] Physics [physics][ PHYS.PHYS.PHYS-OPTICS ] Physics [physics]/Physics [physics]/Optics [physics.optics]Surfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical scienceschemistry[SPI.OPTI]Engineering Sciences [physics]/Optics / PhotonicSurface modification[ SPI.NANO ] Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics[ SPI.OPTI ] Engineering Sciences [physics]/Optics / Photonic0210 nano-technologyLangmuir : the ACS journal of surfaces and colloids
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Quantifying the Covalent Functionalization of Black Phosphorus

2020

Abstract A straightforward quantification method to consistently determine the overall functionalization degree of covalently modified two‐dimensional (2D) black phosphorus (BP) by Raman spectroscopy has been carried out. Indeed, the successful reductive methylation of the BP lattice using sodium intercalation compounds and exhibiting different functionalization degrees has been demonstrated by 31P‐magic angle spinning (MAS) NMR spectroscopy. Furthermore, the correlation of 31P‐MAS NMR spectroscopy and statistical Raman spectroscopy (SRS) revealed the first method to determine the functionalization degree of BP solely by evaluating the intensities of distinct peaks in the Raman spectra of t…

Intercalation (chemistry)reduction010402 general chemistry01 natural sciencesCatalysisBlack phosphoruslaw.inventionCovalent functionalizationsymbols.namesakelawMaterialsResearch Articles010405 organic chemistryGrapheneChemistryGeneral ChemistryNuclear magnetic resonance spectroscopy3. Good health0104 chemical sciencesEspectroscòpia Ramancovalent functionalizationCovalent bondBlack PhosphorusRaman spectroscopyddc:540symbolsSurface modificationPhysical chemistryRaman spectroscopyResearch Article31P-MAS NMR spectroscopy
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Endfunctional Polymers by Functionalization of Living Cationic Chain Ends with 1,1-Diphenylethylene

1995

Abstract A new functionalization method has been developed for the synthesis of 2,2-diphenylvinyl(DPV)-telechelic polyisobutylene (PIB). First, living carbocationic polymerization (LCCP) of isobutylene (IB) is quantitatively end-quenched with a nonpolymerizable olefin, 1,1-diphenylethylene (DPE). This process yields a mixture of diphenyl substituted vinyl and tertiary chlorine endgroups. Treatment of the resulting polymer with potassium-tert-butoxide (tBuOK) leads to the quantitative formation of DPV-telechelic PIB which is a potential macroinitiator precursor for living anionic polymerizations.

Isobutylenechemistry.chemical_classificationOlefin fiberTelechelic polymerPolymers and PlasticsCationic polymerizationChemical modificationGeneral ChemistryPolymerchemistry.chemical_compoundPolymerizationchemistryPolymer chemistryMaterials ChemistryCeramics and CompositesSurface modificationOrganic chemistryJournal of Macromolecular Science, Part A
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Rapid and Complete Surface Modification with Strain-Promoted Oxidation-Controlled Cyclooctyne-1,2-Quinone Cycloaddition (SPOCQ)

2017

Abstract Strain‐promoted oxidation‐controlled cyclooctyne‐1,2‐quinone cycloaddition (SPOCQ) between functionalized bicyclo[6.1.0]non‐4‐yne (BCN) and surface‐bound quinones revealed an unprecedented 100 % conjugation efficiency. In addition, monitoring by direct analysis in real time mass spectrometry (DART‐MS) revealed the underlying kinetics and activation parameters of this immobilization process in dependence on its microenvironment.

Kinetics02 engineering and technologyMetal-free click chemistry010402 general chemistryMass spectrometry01 natural sciencesCatalysisQuímica de superfíciesVLAGMass spectrometryStrain (chemistry)Bicyclic moleculeChemistryCommunicationOrganic ChemistryGeneral MedicineGeneral ChemistryCyclooctynes021001 nanoscience & nanotechnologyOrganische ChemieSurface chemistryCombinatorial chemistryCommunicationsCycloaddition0104 chemical sciencesQuinoneKineticsSurface modification0210 nano-technologyQuímica orgànicaAngewandte Chemie International Edition
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Strain-Promoted Cycloaddition of Cyclopropenes with o-Quinones : A Rapid Click Reaction

2018

Abstract Novel click reactions are of continued interest in fields as diverse as bio‐conjugation, polymer science and surface chemistry. Qualification as a proper “click” reaction requires stringent criteria, including fast kinetics and high conversion, to be met. Herein, we report a novel strain‐promoted cycloaddition between cyclopropenes and o‐quinones in solution and on a surface. We demonstrate the “click character” of the reaction in solution and on surfaces for both monolayer and polymer brush functionalization.

KineticsClick Chemistry | Hot Paper010402 general chemistryPolymer brushO quinones01 natural sciencesCatalysisReaccions químiquesMonolayerotorhinolaryngologic diseasesMetal-free click reactionsVLAGchemistry.chemical_classificationMonolayersMass spectrometry010405 organic chemistryChemistryCommunicationOrganic ChemistryGeneral MedicineGeneral ChemistryPolymerCombinatorial chemistryOrganische ChemieCycloadditionCommunications0104 chemical sciencesKineticsClick chemistrySurface modificationPolymer brushesQuímica orgànicahuman activitiesAngewandte Chemie - International Edition
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Synthesis, characterization and study of covalently modified triazole LAPONITE® edges

2020

Abstract LAPONITE® (Lap) clay mineral was successful functionalized by triazole groups in a two steps procedure. First, the Lap edges were modified with 3-azidopropyltrimethoxysilane by traditional heating and microwave irradiation. Microwave irradiation allowed us to obtain high loading onto the Lap edges in lower times compared to those obtained through conventional method. Afterwards, the triazole moieties were obtained by reaction between azido functionalized Lap and propargyl alcohol. The successful functionalization of Lap was proved by thermogravimetric analysis, FT-IR spectroscopy, dynamic light scattering and ζ-potential measurements. Finally, the effects of the surface modificatio…

LAPONITE® Covalent modification Triazole moieties HydrogelThermogravimetric analysisMaterials scienceTriazole020101 civil engineeringGeology02 engineering and technologySettore CHIM/06 - Chimica OrganicaPropargyl alcohol021001 nanoscience & nanotechnology0201 civil engineeringlaw.inventionchemistry.chemical_compoundchemistryChemical engineeringDynamic light scatteringOptical microscopeGeochemistry and PetrologylawCovalent bondSurface modification0210 nano-technologySpectroscopySettore CHIM/02 - Chimica Fisica
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Interface-Assisted Sign Inversion of Magnetoresistance in Spin Valves Based on Novel Lanthanide Quinoline Molecules

2018

Molecules are proposed to be an efficient medium to host spin-polarized carriers, due to their weak spin relaxation mechanisms. While relatively long spin lifetimes are measured in molecular devices, the most promising route toward device functionalization is to use the chemical versatility of molecules to achieve a deterministic control and manipulation of the electron spin. Here, by combining magnetotransport experiments with element-specific X-ray absorption spectroscopy, this study shows the ability of molecules to modify spin-dependent properties at the interface level via metal–molecule hybridization pathways. In particular, it is described how the formation of hybrid states determine…

LanthanideMaterials scienceCondensed matter physicsMagnetoresistanceSpin polarizationAbsorption spectroscopySpin valve02 engineering and technology021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesElectronic Optical and Magnetic MaterialsBiomaterials0103 physical sciencesElectrochemistryMoleculeSurface modificationCondensed Matter::Strongly Correlated Electrons010306 general physics0210 nano-technologySpin (physics)Materials
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Chemisorption of Atomically Precise 42-Carbon Graphene Quantum Dots on Metal Oxide Films Greatly Accelerates Interfacial Electron Transfer

2019

Graphene quantum dots (GQDs) are emerging as environmentally friendly, low-cost, and highly tunable building blocks in solar energy conversion architectures, such as solar (fuel) cells. Specifically, GQDs constitute a promising alternative for organometallic dyes in sensitized oxide systems. Current sensitized solar cells employing atomically precise GQDs are based on physisorbed sensitizers, with typically limited efficiencies. Chemisorption has been pointed out as a solution to boost photoconversion efficiencies, by allowing improved control over sensitizer surface coverage and sensitizer-oxide coupling strength. Here, employing time-resolved THz spectroscopy, we demonstrate that chemisor…

LetterMaterials scienceGrapheneOxidechemistry.chemical_elementNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundElectron transferchemistryQuantum dotlawChemisorptionSurface modificationGeneral Materials SciencePhysical and Theoretical Chemistry0210 nano-technologyMesoporous materialCarbonThe Journal of Physical Chemistry Letters
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Fluoride-induced modulation of ionic transport in asymmetric nanopores functionalized with “caged” fluorescein moieties

2016

[EN] We demonstrate experimentally and theoretically a nanofluidic fluoride sensing device based on a single conical pore functionalized with "caged" fluorescein moieties. The nanopore functionalization is based on an amine-terminated fluorescein whose phenolic hydroxyl groups are protected with tert-butyldiphenylsilyl (TBDPS) moieties. The protected fluorescein (Fcn-TBDPS-NH2) molecules are then immobilized on the nanopore surface via carbodiimide coupling chemistry. Exposure to fluoride ions removes the uncharged TBDPS moieties due to the fluoride-promoted cleavage of the silicon-oxygen bond, leading to the generation of negatively charged groups on the fluorescein moieties immobilized on…

Life sciences; biologyReaction stepAnalytical chemistryHalideIonic bonding02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundNanoporechemistryddc:570FISICA APLICADASurface modificationMoleculeGeneral Materials ScienceFluorescein0210 nano-technologyFluorideNanoscale
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